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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by OMIM:268130
  • Original References(s): PMID:21477109


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:18252230


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by OMIM:268130


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:18252230, PMID:18979121, PMID:21199492, PMID:21477109, PMID:21536674, PMID:25741868, PMID:29483670


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:28492532, PMID:30311386


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:18669893, PMID:21199492, PMID:28492532


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:18669893, PMID:28492532


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:18669893, PMID:21199492, PMID:22211879, PMID:28492532


  • An association has been curated linking Tinf2 and Revesz syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TINF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Revesz syndrome  (DOID:0070026)
  • 7 papers in RGD have been used to annotate Tinf2
  • Curation Notes: ClinVar Annotator: match by term: Revesz syndrome
  • Original References(s): PMID:26193622, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.